Canonical Allele Identifier: CA1549806478

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60491901T= , CM000667.2:g.60491901T= GRCh38
NC_000005.9:g.59787728T= , CM000667.1:g.59787728T= GRCh37
NC_000005.8:g.59823485T= NCBI36
NG_027957.1:g.1198A=
NG_027957.2:g.37429A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000506510.6:n.70+30150A= (PDE4D)
NR_024617.1:n.711+3478T= (PART1)
NR_028509.1:n.492+3478T= (PART1)
XM_011543472.1:c.-90+30150A= (PDE4D) XP_011541774.1:n.-90+30150A=
NM_001364599.1:c.-90+4238A= (PDE4D) NP_001351528.1:n.-90+4238A=
XM_024446110.1:c.-90+30150A= (PDE4D) XP_024301878.1:n.-90+30150A=
XM_024446112.1:c.-90+30150A= (PDE4D) XP_024301880.1:n.-90+30150A=